Effect of a single bout of exercise on clock gene expression in human leukocyte

2020 ◽  
Vol 128 (4) ◽  
pp. 847-854 ◽  
Author(s):  
Yoshiaki Tanaka ◽  
Hitomi Ogata ◽  
Momoko Kayaba ◽  
Akira Ando ◽  
Insung Park ◽  
...  

Mammals have circadian clocks, which consist of the central clock in the suprachiasmatic nucleus and the peripheral clocks in the peripheral tissues. The effect of exercise on phase of peripheral clocks have been reported in rodents but not in humans. Continuous sampling is necessary to assess the phase of the circadian rhythm of peripheral clock gene expressions. It has been assumed that the expression of the genes in leukocyte may be “an accessible window to the multiorgan transcriptome.” The present study aimed to examine whether exercise affects the level and phase of clock gene expression in human leukocytes. Eleven young men participated in three trials, in which they performed a single bout of exercise at 60% V̇o2max for 1 h beginning either at 0700 (morning exercise) or 1600 (afternoon exercise) or no exercise (control). Blood samples were collected at 0600, 0900, 1200, 1500, 1800, 2100, and 2300 and at 0600 the next morning, to assess diurnal changes of clock gene expression in leukocytes. Brain and muscle ARNT-like protein 1 ( Bmal1) expression level increased after morning and afternoon exercise, and Cryptochrome 1 ( Cry1) expression level increased after morning exercise. Compared with control trial, acrophase of Bmal1 expression tended to be earlier in morning exercise trial and later in afternoon exercise trial. Acrophase of Cry1 expression was earlier in morning exercise trial but not affected by afternoon exercise. Circadian locomotor output cycles kaput ( Clock), Period 1–3 ( Per1–3), and Cry2 expression levels and those acrophases were not affected by exercise. The present results suggest a potential role of a single bout of exercise to modify peripheral clocks in humans. NEW & NOTEWORTHY The present study showed that a single bout of exercise affected peripheral clock gene expression in human leukocytes and the effect of exercise depended on when it was performed. Brain and muscle ARNT-like protein 1 ( Bmal1) expression was increased after exercises performed in the morning and afternoon. Cryptochrome 1 ( Cry1) expression was also increased after the morning exercise. The effect of exercise on acrophase of Bmal1 depended on the time of the exercise: advanced after morning exercise and delayed after afternoon exercise.

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Takafumi Fukuda ◽  
Atsushi Haraguchi ◽  
Mari Kuwahara ◽  
Kaai Nakamura ◽  
Yutaro Hamaguchi ◽  
...  

Hypertension ◽  
2015 ◽  
Vol 66 (2) ◽  
pp. 332-339 ◽  
Author(s):  
Katja Drägert ◽  
Indranil Bhattacharya ◽  
Giovanni Pellegrini ◽  
Petra Seebeck ◽  
Abdelhalim Azzi ◽  
...  

2014 ◽  
Vol 40 (3) ◽  
pp. 295-304 ◽  
Author(s):  
Massimo Bracci ◽  
Nicola Manzella ◽  
Alfredo Copertaro ◽  
Sara Staffolani ◽  
Elisabetta Strafella ◽  
...  

2020 ◽  
Vol 21 (5) ◽  
pp. 1884 ◽  
Author(s):  
Kanami Orihara ◽  
Atsushi Haraguchi ◽  
Shigenobu Shibata

The circadian clock system works not only as a cellular time-keeper but also as a coordinator for almost all physiological functions essential to maintaining human health. Therefore, disruptions or malfunctions of this system can cause many diseases and pre-symptomatic conditions. Indeed, previous studies have indicated that disrupted clock gene expression rhythm is closely related to obesity, and that allergic diseases can be regulated by controlling peripheral clocks in organs and tissues. Moreover, recent studies have found that obesity can lead to immune disorders. Accordingly, in this review, we assess the connection between obesity and allergy from the point of view of the circadian clock system anew and summarize the relationships among the circadian clock system, obesity, and allergy.


Author(s):  
Andreas Schober ◽  
Richard M. Blay ◽  
Saffiyeh Saboor Maleki ◽  
Farima Zahedi ◽  
Anja E. Winklmaier ◽  
...  

Background: The necrotic core partly formed by ineffective efferocytosis increases the risk of an atherosclerotic plaque rupture. microRNAs contribute to necrotic core formation by regulating efferocytosis and macrophage apoptosis. Atherosclerotic plaque rupture occurs at increased frequency in the early morning, indicating diurnal changes in plaque vulnerability. Although circadian rhythms play a role in atherosclerosis, the molecular clock output pathways that control plaque composition and rupture susceptibility are unclear. Methods: Circadian gene expression, necrotic core size, and apoptosis and efferocytosis in aortic lesions were investigated at different times of the day in Apoe -/- Mir21 +/+ mice and Apoe -/- Mir21 -/- mice after consumption of a high-fat diet for 12 weeks feeding. Genome-wide gene expression and lesion formation were analyzed in bone marrow (BM)-transplanted mice. Diurnal changes in apoptosis and clock gene expression were determined in human atherosclerotic lesions. Results: The expression of molecular clock genes, lesional apoptosis, and necrotic core size were diurnally regulated in Apoe -/- mice. Efferocytosis did not match the diurnal increase in apoptosis at the beginning of the active phase. However, in parallel with apoptosis, expression levels of oscillating Mir21 strands decreased in the mouse atherosclerotic aorta. Mir21 knockout abolished circadian regulation of apoptosis and reduced necrotic core size, but did not affect core clock gene expression. Further, Mir21 knockout upregulated expression of pro-apoptotic XIAP associated factor 1 ( Xaf1 ) in the atherosclerotic aorta, which abolished circadian expression of Xaf1. The anti-apoptotic effect of Mir21 was mediated by non-canonical targeting of Xaf1 through both Mir21 strands. Mir21 knockout in BM cells also reduced atherosclerosis and necrotic core size. Circadian regulation of clock gene expression was confirmed in human atherosclerotic lesions. Apoptosis oscillated diurnally in phase with XAF1 expression, demonstrating an early morning peak anti-phase to that of the Mir21 strands. Conclusions: Our findings suggest that the molecular clock in atherosclerotic lesions induces a diurnal rhythm of apoptosis regulated by circadian Mir21 expression in macrophages that is not matched by efferocytosis, thus increasing the size of the necrotic core.


PLoS ONE ◽  
2013 ◽  
Vol 8 (3) ◽  
pp. e59808 ◽  
Author(s):  
Susan Westfall ◽  
Argel Aguilar-Valles ◽  
Valérie Mongrain ◽  
Giamal N. Luheshi ◽  
Nicolas Cermakian

2018 ◽  
Vol 52 ◽  
pp. 1-6 ◽  
Author(s):  
Kamila Weissová ◽  
Jitka Škrabalová ◽  
Kateřina Skálová ◽  
Kateřina Červená ◽  
Zdeňka Bendová ◽  
...  

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